-
1
-
-
0007010412
-
Antiretroviral therapy for HIV infections in 1998
-
Carpenter, C. C. J.; Fischl, M. A.; Hammer, S. M.; Hirsch, M. S.; Jacobsen, D. M.; Katzenstein, D. A.; Montaner, J. S. G.; Richman, D. D.; Saag, M. S.; Schooley, R. T.; Thompson, M. A.; Vella, S.; Yeni, P. G.; Volberding, P. A. Antiretroviral Therapy for HIV Infections in 1998. J. Am. Med. Assoc. 1998, 280, 78-86.
-
(1998)
J. Am. Med. Assoc.
, vol.280
, pp. 78-86
-
-
Carpenter, C.C.J.1
Fischl, M.A.2
Hammer, S.M.3
Hirsch, M.S.4
Jacobsen, D.M.5
Katzenstein, D.A.6
Montaner, J.S.G.7
Richman, D.D.8
Saag, M.S.9
Schooley, R.T.10
Thompson, M.A.11
Vella, S.12
Yeni, P.G.13
Volberding, P.A.14
-
2
-
-
0032437454
-
The role of non-nucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection
-
De Clercq, E. The Role of Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) in the Therapy of HIV-1 Infection. Antiviral Res. 1998, 38, 153-179.
-
(1998)
Antiviral Res.
, vol.38
, pp. 153-179
-
-
De Clercq, E.1
-
3
-
-
0008782655
-
Report of the NIH panel to define principles of therapy of HIV infection and guidelines for the use of antiretroviral agents in HIV-infected adults and adolescents
-
Report of the NIH Panel to Define Principles of Therapy of HIV Infection and Guidelines for the Use of Antiretroviral Agents in HIV-Infected Adults and Adolescents. Ann. Int. Med. 1998, 128, 1057-1099.
-
(1998)
Ann. Int. Med.
, vol.128
, pp. 1057-1099
-
-
-
4
-
-
0033014605
-
Guide to major clinical trials of antiretroviral therapy in human immunodeficiency virus-infected patients: Protease inhibitors, non-nucleoside reverse transcriptase inhibitors, and nucleoside reverse transcriptase inhihitors
-
Tavel, J. A.; Miller, K. D.; Masur, H. Guide to Major Clinical Trials of Antiretroviral Therapy in Human Immunodeficiency Virus-Infected Patients: Protease Inhibitors, Non-Nucleoside Reverse Transcriptase Inhibitors, and Nucleoside Reverse Transcriptase Inhihitors. Clin. Infect. Dis. 1999, 28, 643-676.
-
(1999)
Clin. Infect. Dis.
, vol.28
, pp. 643-676
-
-
Tavel, J.A.1
Miller, K.D.2
Masur, H.3
-
5
-
-
0028860918
-
Synthesis and biological evaluation of an alkenyldiarylmethane (ADAM) which acts as a novel nonnucleoside HIV-1 reverse transcriptase inhibitor
-
Cushman, M.; Golebiewski, M.; Buckheit, R. W. J.; Graham, L.; Rice, W. G. Synthesis and Biological Evaluation of an Alkenyldiarylmethane (ADAM) which Acts as a Novel Nonnucleoside HIV-1 Reverse Transcriptase Inhibitor. Bioorg. Med. Chem. Lett. 1995, 5, 2713-2716.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 2713-2716
-
-
Cushman, M.1
Golebiewski, M.2
Buckheit, R.W.J.3
Graham, L.4
Rice, W.G.5
-
6
-
-
0029783936
-
Synthesis and biological evaluation of certain alkenyldiarylmethanes as anti-HIV-1 agents which act as non-nucleoside reverse transcriptase inhibitors
-
Cushman, M.; Golebiewski, W. M.; Graham, L.; Turpin, J. A.; Rice, W. G.; Fliakas-Boltz, V.; Buckheit, R. W. J. Synthesis and Biological Evaluation of Certain Alkenyldiarylmethanes as Anti-HIV-1 Agents Which Act as Non-Nucleoside Reverse Transcriptase Inhibitors. J. Med. Chem. 1996, 39, 3217-3227.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 3217-3227
-
-
Cushman, M.1
Golebiewski, W.M.2
Graham, L.3
Turpin, J.A.4
Rice, W.G.5
Fliakas-Boltz, V.6
Buckheit, R.W.J.7
-
7
-
-
0032548456
-
Synthesis of a non-nucleoside reverse transcriptase inhibitor in the alkenyldiarylmethane (ADAM) series with optimized potency and therapeutic index
-
Cushman, M.; Casimiro-Garcia, A.; Williamson, K.; Rice, W. G. Synthesis of a Non-Nucleoside Reverse Transcriptase Inhibitor in the Alkenyldiarylmethane (ADAM) Series with Optimized Potency and Therapeutic Index. Bioorg. Med. Chem. Lett. 1998, 8, 195-198.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 195-198
-
-
Cushman, M.1
Casimiro-Garcia, A.2
Williamson, K.3
Rice, W.G.4
-
8
-
-
0032482316
-
New alkenyldiarylmethanes with enhanced potencies as anti-HIV agents which act as non-nucleoside reverse transcriptase inhibitors
-
Cushman, M.; Casimiro-Garcia, A.; Hejchman, E.; Ruell, J. A.; Huang, M.; Schaeffer, C. A.; Williamson, K.; Rice, W. G.; Buckheit, R. W. J. New Alkenyldiarylmethanes with Enhanced Potencies as Anti-HIV Agents Which Act as Non-Nucleoside Reverse Transcriptase Inhibitors. J. Med. Chem. 1998, 41, 2076-2089.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2076-2089
-
-
Cushman, M.1
Casimiro-Garcia, A.2
Hejchman, E.3
Ruell, J.A.4
Huang, M.5
Schaeffer, C.A.6
Williamson, K.7
Rice, W.G.8
Buckheit, R.W.J.9
-
9
-
-
0344158928
-
-
Unpublished results
-
Casimiro-Garcia, A.; De Clercq, E.; Pannecouque, C.; Witvrouw, M.; Stup, T. L.; Turpin, J. A.; Buckheit, R. W. J.; Cushman, M. Synthesis and Anti-HIV Activity of Cosalane Analogues Incorporating Nitrogen in the Linker Chain. Unpublished results, 1999.
-
(1999)
Synthesis and Anti-HIV Activity of Cosalane Analogues Incorporating Nitrogen in the Linker Chain
-
-
Casimiro-Garcia, A.1
De Clercq, E.2
Pannecouque, C.3
Witvrouw, M.4
Stup, T.L.5
Turpin, J.A.6
Buckheit, R.W.J.7
Cushman, M.8
-
10
-
-
0027996494
-
Design, synthesis, and biological evaluation of cosalane, a novel anti-HIV agent which inhibits multiple features of virus replication
-
Cushman, M.; Golebiewski, W. M.; McMahon, J. B.; Buckheit, R. W. J.; Clanton, D. J.; Weislow, O.; Haugwitz, R. D.; Bader, J.; Graham, L.; Rice, W. G. Design, Synthesis, and Biological Evaluation of Cosalane, a Novel anti-HIV Agent which Inhibits Multiple Features of Virus Replication. J. Med. Chem. 1994, 37, 3040-3050.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3040-3050
-
-
Cushman, M.1
Golebiewski, W.M.2
McMahon, J.B.3
Buckheit, R.W.J.4
Clanton, D.J.5
Weislow, O.6
Haugwitz, R.D.7
Bader, J.8
Graham, L.9
Rice, W.G.10
-
11
-
-
0344590520
-
Studies related to naturally occurring acetylenic compounds. XXXIII. A preliminary investigation of Coreopsis gigantea
-
Sorensen, S. J.; Soransen, N. A. Studies Related to Naturally Occurring Acetylenic Compounds. XXXIII. A Preliminary Investigation of Coreopsis gigantea. Acta Chem. Scand. 1966, 20, 992-1002.
-
(1966)
Acta Chem. Scand.
, vol.20
, pp. 992-1002
-
-
Sorensen, S.J.1
Soransen, N.A.2
-
12
-
-
0003054921
-
A rapid, mild procedure for the preparation of alkyl chlorides and bromides
-
Hooz, J.; Giliani, H. H. S. A Rapid, Mild Procedure for the Preparation of Alkyl Chlorides and Bromides. Can. J. Chem. 1968, 46, 86-87.
-
(1968)
Can. J. Chem.
, vol.46
, pp. 86-87
-
-
Hooz, J.1
Giliani, H.H.S.2
-
13
-
-
0017391169
-
A synthesis of (±)-methyl n-tetradeca-trans-2,2,5-trienoate, an allenic ester produced by the male dried bean beetle Acanthoscelodes obtectus (say)
-
Kocienski, P. J.; Cernigliaro, G.; Feldstein, G. A Synthesis of (±)-Methyl n-Tetradeca-trans-2,2,5-trienoate, an Allenic Ester Produced by the Male Dried Bean Beetle Acanthoscelodes obtectus (Say). J. Org. Chem. 1977, 42, 353-355.
-
(1977)
J. Org. Chem.
, vol.42
, pp. 353-355
-
-
Kocienski, P.J.1
Cernigliaro, G.2
Feldstein, G.3
-
14
-
-
0344590518
-
-
Paquette, L. A., Ed.; John Wiley and Sons: New York
-
Vaillancourt, V.; Cudahy, M. M. In Encyclopedia of Reagents for Organic Synthesis; Paquette, L. A., Ed.; John Wiley and Sons: New York, 1995; Vol. 5, pp 3307-3311.
-
(1995)
Encyclopedia of Reagents for Organic Synthesis
, vol.5
, pp. 3307-3311
-
-
Vaillancourt, V.1
Cudahy, M.M.2
-
15
-
-
0011878207
-
Acylation by ketenes and isocyanates. A mechanistic comparison
-
Satchell, D. P. N.; Satchell, R. S. Acylation by Ketenes and Isocyanates. A Mechanistic Comparison. Chem. Soc. Rev. 1975, 4, 231-250.
-
(1975)
Chem. Soc. Rev.
, vol.4
, pp. 231-250
-
-
Satchell, D.P.N.1
Satchell, R.S.2
-
16
-
-
0030749916
-
Design, synthesis, and biological evaluation of new growth inhibitors of trypanosoma cruzi (epimastigotes)
-
Schartzapel, A. J.; Zhong, L.; Docampo, R.; Rodriguez, J. B.; Gros, E. G. Design, Synthesis, and Biological Evaluation of New Growth Inhibitors of Trypanosoma cruzi (Epimastigotes). J. Med. Chem. 1987, 40, 2314-2322.
-
(1987)
J. Med. Chem.
, vol.40
, pp. 2314-2322
-
-
Schartzapel, A.J.1
Zhong, L.2
Docampo, R.3
Rodriguez, J.B.4
Gros, E.G.5
-
17
-
-
84989478646
-
Activated dimethyl sulfoxide: Useful reagents for synthesis
-
Mancuso, A. J.; Swern, D. Activated Dimethyl Sulfoxide: Useful Reagents for Synthesis. Synthesis 1981, 165-185.
-
(1981)
Synthesis
, pp. 165-185
-
-
Mancuso, A.J.1
Swern, D.2
-
18
-
-
4243973410
-
Carbonyl-coupling reactions using low-valent titanium
-
McMurry, J. E. Carbonyl-Coupling Reactions Using Low-Valent Titanium. Chem. Rev. 1989, 89, 1513-1524.
-
(1989)
Chem. Rev.
, vol.89
, pp. 1513-1524
-
-
McMurry, J.E.1
-
19
-
-
0030444646
-
New developments in the chemistry of low valent titanium
-
Fürstner, A.; Bogdavovic, B. New Developments in the Chemistry of Low Valent Titanium. Angew. Chem., Int. Ed. Engl. 1996, 35, 2442-469.
-
(1996)
Angew. Chem., Int. Ed. Engl.
, vol.35
, pp. 2442-2469
-
-
Fürstner, A.1
Bogdavovic, B.2
-
20
-
-
0000442177
-
Antipsoriatic anthrones with modulated redox properties. 4. Synthesis and biological activity of novel 9.10-dihydro-1,8-dihydroxy-9-oxo-2-anthracenecarboxylic and -hydroxamin acids
-
Müller, K.; Prinz, H. Antipsoriatic Anthrones with Modulated Redox Properties. 4. Synthesis and Biological Activity of Novel 9.10-Dihydro-1,8-dihydroxy-9-oxo-2-anthracenecarboxylic and -hydroxamin Acids. J. Med. Chem. 1997, 40, 2780-2787.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2780-2787
-
-
Müller, K.1
Prinz, H.2
-
21
-
-
0001018230
-
Preparation of functionalized ketones via low-temperature grignard reaction
-
Eberle, M. K.; Kahle, G. G. Preparation of Functionalized Ketones via Low-Temperature Grignard Reaction. Tetrahedron Lett. 1980, 21, 2303-2304.
-
(1980)
Tetrahedron Lett.
, vol.21
, pp. 2303-2304
-
-
Eberle, M.K.1
Kahle, G.G.2
-
22
-
-
0000376544
-
Enantioselective total synthesis of a protosterol, 3b,20-dihydroxyprotost-24-ene
-
Corey, E. J.; Virgil, S. C. Enantioselective Total Synthesis of a Protosterol, 3b,20-Dihydroxyprotost-24-ene. J. Am. Chem. Soc. 1990, 112, 6429-6431.
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 6429-6431
-
-
Corey, E.J.1
Virgil, S.C.2
-
23
-
-
4244096024
-
Pyridinium tosylate, a mild catalyst for formation and cleavage of dioxolane-type acetals
-
Sterzycki, R. Pyridinium Tosylate, a Mild Catalyst for Formation and Cleavage of Dioxolane-Type Acetals. Synthesis 1979, 724-725.
-
(1979)
Synthesis
, pp. 724-725
-
-
Sterzycki, R.1
-
24
-
-
84985199461
-
A Convenient method of preparing the leukotriene precursor methyl 5-oxopentanoate
-
Huckstep, M.; Taylor, R. J. K. A Convenient Method of Preparing the Leukotriene Precursor Methyl 5-Oxopentanoate. Synthesis 1982, 881-882.
-
(1982)
Synthesis
, pp. 881-882
-
-
Huckstep, M.1
Taylor, R.J.K.2
-
25
-
-
4243468938
-
The cation-π interaction
-
Ma, J. C.; Dougherty, D. A. The Cation-π Interaction. Chem. Rev. 1997, 97, 1303-1324.
-
(1997)
Chem. Rev.
, vol.97
, pp. 1303-1324
-
-
Ma, J.C.1
Dougherty, D.A.2
-
26
-
-
0032558123
-
Energetic analysis of an engineered cation-π interaction in staphylococcal nuclease
-
Ting, A. Y.; Shin, I.; Lucero, C.; Schultz, P. G. Energetic Analysis of an Engineered Cation-π Interaction in Staphylococcal Nuclease. J. Am. Chem. Soc. 1998, 120, 7135-7136.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 7135-7136
-
-
Ting, A.Y.1
Shin, I.2
Lucero, C.3
Schultz, P.G.4
-
28
-
-
0025014499
-
Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives
-
Pauwels, R.; Andries, K.; Desmyter, J.; Schols, D.; Kukla, M. J.; Breslin, H. J.; Raeymaeckers, A.; Van Gelder, J.; Woestenborghs, R.; Heykants, J.; Schellekens, K.; Janssen, M. A. C.; De Clercq, E.; Janssen, P. A. J. Potent and Selective Inhibition of HIV-1 Replication In Vitro by a Novel Series of TIBO Derivatives. Nature 1990, 343, 470-474.
-
(1990)
Nature
, vol.343
, pp. 470-474
-
-
Pauwels, R.1
Andries, K.2
Desmyter, J.3
Schols, D.4
Kukla, M.J.5
Breslin, H.J.6
Raeymaeckers, A.7
Van Gelder, J.8
Woestenborghs, R.9
Heykants, J.10
Schellekens, K.11
Janssen, M.A.C.12
De Clercq, E.13
Janssen, P.A.J.14
-
29
-
-
0026030735
-
Potent and selective inhibition of human immunodeficiency virus type 1 (HIV-1) by 5-ethyl-6-phenylthiouracil derivatives through their interaction with the HIV-1 reverse transcriptase
-
Baba, M.; De Clercq, E.; Tanaka, H.; Ubasawa, M.; Takashima, H.; Sekiya, K.; Nitta, I.; Umezu, K.; Nakashima, H.; Mon, S.; Shigeta, S.; Walker, R. T.; Miyasaka, T. Potent and Selective Inhibition of Human Immunodeficiency Virus Type 1 (HIV-1) by 5-Ethyl-6-phenylthiouracil Derivatives through Their Interaction with the HIV-1 Reverse Transcriptase. Proc. Natl. Acad. Sci. U.S.A. 1991, 88, 2356-2360.
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, pp. 2356-2360
-
-
Baba, M.1
De Clercq, E.2
Tanaka, H.3
Ubasawa, M.4
Takashima, H.5
Sekiya, K.6
Nitta, I.7
Umezu, K.8
Nakashima, H.9
Mon, S.10
Shigeta, S.11
Walker, R.T.12
Miyasaka, T.13
-
30
-
-
0025962924
-
An antiviral target on reverse transcriptase of human immunodeficiency virus type 1 revealed by tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one and -thione derivatives
-
Debyser, Z.; Pauwels, R.; Andries, K.; Desmyter, J.; Kukla, M.; Janssen, P. A. J.; De Clercq, E. An Antiviral Target on Reverse Transcriptase of Human Immunodeficiency Virus Type 1 Revealed by Tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one and -thione Derivatives. Proc. Natl. Acad. Sci. U.S.A. 1991, 88, 1451-1455.
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, pp. 1451-1455
-
-
Debyser, Z.1
Pauwels, R.2
Andries, K.3
Desmyter, J.4
Kukla, M.5
Janssen, P.A.J.6
De Clercq, E.7
-
31
-
-
0026724892
-
Kinetics of inhibition of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase analogue [2′,5′-Bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]- 3′-spiro-5″-(4″-amino-1″,2″-oxathiole-2″, 2″-dioxide)thymine (TSAO-T)
-
Balzarini, J.; Pérez-Pérez, M.-J.; San-Félix, A.; Camarasa, M.-J.; Bathurst, I. C.; Barr, P. J.; De Clercq, E. Kinetics of Inhibition of Human Immunodeficiency Virus Type 1 (HIV-1) Reverse Transcriptase Analogue [2′,5′-Bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]- 3′-spiro-5″-(4″-amino-1″,2″-oxathiole-2″, 2″-dioxide)thymine (TSAO-T). J. Biol. Chem. 1992, 267, 11831.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 11831
-
-
Balzarini, J.1
Pérez-Pérez, M.-J.2
San-Félix, A.3
Camarasa, M.-J.4
Bathurst, I.C.5
Barr, P.J.6
De Clercq, E.7
-
32
-
-
0026014455
-
A TIBO derivative, R82913, is a potent inhibitor of HIV-1 reverse transcriptase with heteropolymer templates
-
White, E. L.; Buckheit, R. W. J.; Ross, L. J.; Germany, J. M.; Andries, K.; Pauwels, R.; Janssen, P. A.; Shannon, W. M.; Chirigos, M. A. A TIBO Derivative, R82913, is a Potent Inhibitor of HIV-1 Reverse Transcriptase with Heteropolymer Templates. Antiviral Res. 1991, 16, 257-266.
-
(1991)
Antiviral Res.
, vol.16
, pp. 257-266
-
-
White, E.L.1
Buckheit, R.W.J.2
Ross, L.J.3
Germany, J.M.4
Andries, K.5
Pauwels, R.6
Janssen, P.A.7
Shannon, W.M.8
Chirigos, M.A.9
-
33
-
-
0028947588
-
High-resolution sturctures of HIV-1 RT from four RT-inhibitor complexes
-
Ren, J.; Esnouf, R.; Garman, E.; Somers, D.; Ross, C.; Kirby, I.; Keeling, J.; Darby, G.; Jones, Y.; Stuart, D.; Stammers, D. High-Resolution Sturctures of HIV-1 RT from Four RT-Inhibitor Complexes. Struct. Biol. 1995, 2, 293-302.
-
(1995)
Struct. Biol.
, vol.2
, pp. 293-302
-
-
Ren, J.1
Esnouf, R.2
Garman, E.3
Somers, D.4
Ross, C.5
Kirby, I.6
Keeling, J.7
Darby, G.8
Jones, Y.9
Stuart, D.10
Stammers, D.11
-
34
-
-
0029075207
-
Structure of HIV-1 RT/TIBO R 86183 complex reveals similarity in the binding of diverse nonnucleoside inhibitors
-
Ding, J.; Das, K.; Moereels, H.; Koymans, L.; Andries, K.; Janssen, P. A.; Hughes, S. H.; Arnold, E. Structure of HIV-1 RT/TIBO R 86183 Complex Reveals Similarity in the Binding of Diverse Nonnucleoside Inhibitors. Nature Struct. Biol. 1995, 2, 407-415.
-
(1995)
Nature Struct. Biol.
, vol.2
, pp. 407-415
-
-
Ding, J.1
Das, K.2
Moereels, H.3
Koymans, L.4
Andries, K.5
Janssen, P.A.6
Hughes, S.H.7
Arnold, E.8
-
35
-
-
0027528503
-
Non-nucleoside inhibitors of HIV-1 reverse transcriptase: Molecular modeling and x-ray structure investigations
-
Schäfer, W.; Friebe, W.-G.; Leinert, W.; Mertens, A.; Poll, T.; von der Saal, W.; Zilch, H.; Nuber, H.; Ziegler, M. L. Non-Nucleoside Inhibitors of HIV-1 Reverse Transcriptase: Molecular Modeling and X-ray Structure Investigations. J. Med. Chem. 1993, 36, 726-732.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 726-732
-
-
Schäfer, W.1
Friebe, W.-G.2
Leinert, W.3
Mertens, A.4
Poll, T.5
Von Der Saal, W.6
Zilch, H.7
Nuber, H.8
Ziegler, M.L.9
-
36
-
-
0029645409
-
The structure of HIV-1 reverse transcriptase complexed with 9-chloro-TIBO: Lessons for inhibitor design
-
Ren, J.; Esnouf, R.; Hopkins, A.; Ross, C.; Jones, Y.; Stammers, D.; Stuart, D. The structure of HIV-1 Reverse Transcriptase Complexed with 9-Chloro-TIBO: Lessons for Inhibitor Design. Structure 1995, 3, 915-926.
-
(1995)
Structure
, vol.3
, pp. 915-926
-
-
Ren, J.1
Esnouf, R.2
Hopkins, A.3
Ross, C.4
Jones, Y.5
Stammers, D.6
Stuart, D.7
-
37
-
-
13144282707
-
Structures of Tyr 1998Leu mutant and wild-type HIV-1 reverse transcriptase complexed with the non-nucleoside inhibitor HBY 097: Inhibitor flexibility is a useful disign feature for reducing drug resistance
-
Hsiou, Y.; Das, K.; Ding, J.; Clark, A. D. J.; Kleim, J.-P.; Rosner, M.; Winkler, I.; Reiss, G.; Hughes, S. H.; Arnold, E. Structures of Tyr 1998Leu Mutant and Wild-Type HIV-1 Reverse Transcriptase Complexed with the Non-Nucleoside Inhibitor HBY 097: Inhibitor Flexibility is a Useful Disign Feature for Reducing Drug Resistance. J. Mol. Biol. 1998, 284, 313-323.
-
(1998)
J. Mol. Biol.
, vol.284
, pp. 313-323
-
-
Hsiou, Y.1
Das, K.2
Ding, J.3
Clark, A.D.J.4
Kleim, J.-P.5
Rosner, M.6
Winkler, I.7
Reiss, G.8
Hughes, S.H.9
Arnold, E.10
-
38
-
-
0028172345
-
Locations of anti-AIDS drug binding sites and resistance mutations in the three-dimensional structure of HIV-1 reverse transcriptase
-
Tantillo, C.; Ding, J.; Jacobo-Molina, A.; Nanni, R. G.; Boyer, P. L.; Hughes, S. H.; Pauwels, R.; Andries, K.; Janssen, P. A.; Arnold, E. Locations of Anti-AIDS Drug Binding Sites and Resistance Mutations in the Three-dimensional Structure of HIV-1 Reverse Transcriptase. J. Mol. Biol. 1994, 243, 369-387.
-
(1994)
J. Mol. Biol.
, vol.243
, pp. 369-387
-
-
Tantillo, C.1
Ding, J.2
Jacobo-Molina, A.3
Nanni, R.G.4
Boyer, P.L.5
Hughes, S.H.6
Pauwels, R.7
Andries, K.8
Janssen, P.A.9
Arnold, E.10
-
39
-
-
0028271687
-
Structure of the binding site for nonnucleoside inhibitors of the reverse transcriptase of human immunodeficiency type I
-
Smerdon, S. J.; Jäger, J.; Wang, J.; Kohlstaedt, L. A.; Chirino, A. J.; Friedman, J. M.; Rice, P. A.; Steitz, T. A. Structure of the Binding Site for Nonnucleoside Inhibitors of the Reverse Transcriptase of Human Immunodeficiency Type I. Proc. Natl. Acad. Sci. U.S.A. 1994, 91, 3911-3915.
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 3911-3915
-
-
Smerdon, S.J.1
Jäger, J.2
Wang, J.3
Kohlstaedt, L.A.4
Chirino, A.J.5
Friedman, J.M.6
Rice, P.A.7
Steitz, T.A.8
-
40
-
-
0026693137
-
Crystal structure at 3.5 Å resolution of HIV-1 reverse transcriptase complexed with an inhibitor
-
Kohlstaedt, L. A.; Wang, J.; Friedman, J. M.; Rice, P. A.; Steitz, T. A. Crystal Structure at 3.5 Å Resolution of HIV-1 Reverse Transcriptase Complexed with an Inhibitor. Science 1992, 256, 1783-1790.
-
(1992)
Science
, vol.256
, pp. 1783-1790
-
-
Kohlstaedt, L.A.1
Wang, J.2
Friedman, J.M.3
Rice, P.A.4
Steitz, T.A.5
-
41
-
-
0029644484
-
Structure of HIV-1 reverse transcriptase in a complex with the nonnucleoside inhibitor α-APA R 95845 at 2.8 A resolution
-
Ding, J.; Das, K.; Tantillo, C.; Zhang, W.; Clark, A. D. J.; Jessen, S.; Lu, X.; Hsiou, Y.; Jacobo-Molina, A.; Andries, K.; Pauwels, R.; Moereels, H.; Koymans, L.; Janssen, P. A. J.; Smith, R. H. J.; Koepke, M. K.; Michejda, C. J.; Hughes, S. H.; Arnold, E. Structure of HIV-1 Reverse Transcriptase in a Complex with the Nonnucleoside Inhibitor α-APA R 95845 at 2.8 A Resolution. Structure 1995, 3, 365-379.
-
(1995)
Structure
, vol.3
, pp. 365-379
-
-
Ding, J.1
Das, K.2
Tantillo, C.3
Zhang, W.4
Clark, A.D.J.5
Jessen, S.6
Lu, X.7
Hsiou, Y.8
Jacobo-Molina, A.9
Andries, K.10
Pauwels, R.11
Moereels, H.12
Koymans, L.13
Janssen, P.A.J.14
Smith, R.H.J.15
Koepke, M.K.16
Michejda, C.J.17
Hughes, S.H.18
Arnold, E.19
-
42
-
-
0029877789
-
Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) for the treatment of Human Immunodeficiency Virus Type 1 (HIV-1) infections: Strategies to overcome drug resistance development
-
De Clercq, E. Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) for the Treatment of Human Immunodeficiency Virus Type 1 (HIV-1) Infections: Strategies to Overcome Drug Resistance Development. Med. Res. Rev. 1996, 16, 125-157.
-
(1996)
Med. Res. Rev.
, vol.16
, pp. 125-157
-
-
De Clercq, E.1
-
43
-
-
0028029961
-
New tetrahydroimidazo[4,5,1-jk][1,4]-benzodiazepin-2(1H)-one and -thione derivatives are potent inhibitors of human immunodeficiency virus type 1 replication and are synergistic with 2′,3′-dideoxynucleoside analogues
-
Pauwels, R.; Andries, K.; Debyser, Z.; Kukla, M. J.; Schols, D.; Breslin, H. J.; Woestenborghs, R.; Desmyter, J.; Janssen, M. A. C.; De Clercq, E.; Janssen, P. A. J. New Tetrahydroimidazo[4,5,1-jk][1,4]-Benzodiazepin-2(1H)-One and -Thione Derivatives are Potent Inhibitors of Human Immunodeficiency Virus Type 1 Replication and are Synergistic with 2′,3′-Dideoxynucleoside Analogues. Antimicrob. Agents Cehmother. 1994, 38, 2863-2870.
-
(1994)
Antimicrob. Agents Cehmother.
, vol.38
, pp. 2863-2870
-
-
Pauwels, R.1
Andries, K.2
Debyser, Z.3
Kukla, M.J.4
Schols, D.5
Breslin, H.J.6
Woestenborghs, R.7
Desmyter, J.8
Janssen, M.A.C.9
De Clercq, E.10
Janssen, P.A.J.11
-
44
-
-
0027213264
-
A nonnucleoside reverse transcriptase inhibitor active on human immunodeficiency virus type 1 isolates resistant to related inhibitors
-
Goldman, M. E.; O'Brien, J. A.; Ruffing, T. L.; Schlief, W. A.; Sardana, V. V.; Byrnes, V. W.; Condra, J. H.; Hoffman, J. M.; Emini, E. A. A Nonnucleoside Reverse Transcriptase Inhibitor Active on Human Immunodeficiency Virus Type 1 Isolates Resistant to Related Inhibitors. Antimicrob. Agents Chemother. 1993, 37, 947-949.
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 947-949
-
-
Goldman, M.E.1
O'Brien, J.A.2
Ruffing, T.L.3
Schlief, W.A.4
Sardana, V.V.5
Byrnes, V.W.6
Condra, J.H.7
Hoffman, J.M.8
Emini, E.A.9
-
45
-
-
0030596068
-
Crystal structure of 8-Cl and 9-Cl TIBO complexed with wild-type HIV-1 RT and 8-Cl TIBO complexed with the Tyr 181Cys HIV-1 RT drug-resistant mutant
-
Das, K; Ding, J.; Hsiou, Y.; Clark, A. D. J.; Moereels, H.; Koymans, L.; Adries, K.; Pauwels, R.; Janssen, P. A. J.; Boyer, P. L.; Clark, P.; Smith, R. H. J.; Smith, M. B. K.; Michejda, C. J.; Hughes, S. H.; Arnold, E. Crystal Structure of 8-Cl and 9-Cl TIBO Complexed with Wild-type HIV-1 RT and 8-Cl TIBO Complexed with the Tyr 181Cys HIV-1 RT Drug-resistant Mutant. J. Mol. Biol. 1996, 264, 1085-1100.
-
(1996)
J. Mol. Biol.
, vol.264
, pp. 1085-1100
-
-
Das, K.1
Ding, J.2
Hsiou, Y.3
Clark, A.D.J.4
Moereels, H.5
Koymans, L.6
Adries, K.7
Pauwels, R.8
Janssen, P.A.J.9
Boyer, P.L.10
Clark, P.11
Smith, R.H.J.12
Smith, M.B.K.13
Michejda, C.J.14
Hughes, S.H.15
Arnold, E.16
-
46
-
-
0029976422
-
Complexes of HIV-1 reverse transcriptase with inhibitors of the HEPT series reveal conformational changes relavant to the design of potent non-nucleoside inhibitors
-
Hopkins, A. L.; Ren, J.; Esnouf, R. M.; Willcox, B. E.; Jones, E. Y.; Ross, C.; Miyasaka, T.; Walker, R. T.; Tanaka, H.; Stammers, D. K; Stuart, D. I. Complexes of HIV-1 Reverse Transcriptase with Inhibitors of the HEPT Series Reveal Conformational Changes Relavant to the Design of Potent Non-Nucleoside Inhibitors. J. Med. Chem. 1996, 39, 1589-1600.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1589-1600
-
-
Hopkins, A.L.1
Ren, J.2
Esnouf, R.M.3
Willcox, B.E.4
Jones, E.Y.5
Ross, C.6
Miyasaka, T.7
Walker, R.T.8
Tanaka, H.9
Stammers, D.K.10
Stuart, D.I.11
-
47
-
-
0029445163
-
Discovery and in vitro development of AIDS antiviral drugs as biopharmaceuticals
-
Rice, W. G.; Bader, J. P. Discovery and in Vitro Development of AIDS Antiviral Drugs as Biopharmaceuticals. Adv. Pharmacol. (San Diego) 1995, 6, 389-438.
-
(1995)
Adv. Pharmacol. (San Diego)
, vol.6
, pp. 389-438
-
-
Rice, W.G.1
Bader, J.P.2
-
48
-
-
0028838466
-
Structure-activity and cross-resistance evaluations of a series of human immunodeficiency virus type 1-specific compounds related to oxathiin carboxanilide
-
Buckheit, R. W. J.; Kinjerski, T. L.; Fliakas-Boltz, V.; Russell, J. D.; Stup, T. L.; Pallansch, L. A.; Brouwer, W. G.; Dao, D. C.; Harrison, W. A.; Schultz, R. J.; Bader, J. P.; Yang, S. S. Structure-Activity and Cross-Resistance Evaluations of a Series of Human Immunodeficiency Virus Type 1-Specific Compounds Related to Oxathiin Carboxanilide. Antimicrob. Agents Chemother. 1995, 39, 2718-2727.
-
(1995)
Antimicrob. Agents Chemother.
, vol.39
, pp. 2718-2727
-
-
Buckheit, R.W.J.1
Kinjerski, T.L.2
Fliakas-Boltz, V.3
Russell, J.D.4
Stup, T.L.5
Pallansch, L.A.6
Brouwer, W.G.7
Dao, D.C.8
Harrison, W.A.9
Schultz, R.J.10
Bader, J.P.11
Yang, S.S.12
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